{
    "disease_id": "DOID:0070254", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "MOGS-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "CDG IIb"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "CDG syndrome type IIb"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "congenital disorder of glycosylation, type IIb; CDG2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "congenital disorder of glycosylation type 2b"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "GCS1-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "congenital disorder of glycosylation, type IIb"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "glucosidase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "carbohydrate deficient glycoprotein syndrome type IIb"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "CDG-IIb"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "MOGS-CDG (CDG-IIb)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "CDG2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011629", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011629", 
            "name": "CDG 2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070254", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070254", 
            "name": "CDG IIb"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070254", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070254", 
            "name": "CDG2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070254", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070254", 
            "name": "CDGIIb"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070254", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070254", 
            "name": "glucosidase I deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070254", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of MOGS on chromosome 2p13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070254", 
        "name": "congenital disorder of glycosylation type IIb"
    }, 
    "evidence": [
        {
            "url": "https://glycosmos.org/glycogenes/show?source=kegg&gene_id=7841", 
            "id": "7841", 
            "database": "GlyCosmos"
        }
    ]
}
